NCT06573190Completed
Liver Status and Presence of MASLD/MASH in Patients With Chronic Hepatitis B
The Value of Fibroscan® in Assessing the Liver Status and Presence of MASLD/MASH in Patients With Chronic Hepatitis B and Monitoring Changes by Antiviral Therapy: Faraday Study
Source: ClinicalTrials.gov · Last updated 27 Aug 2024
Brief summary (registry, in English)
The aim of the study was to evaluate the consistency between liver biopsy and Liver Stiffness Measurement (LSM) for fibrosis and controlled attenuation parameter (CAP) for steatosis in FibroScan® in patients with chronic hepatitis B. The secondary aim of the study was to demonstrate the efficacy of FibroScan® for following the CHB patients at 12th month of antiviral therapy. The study was prospectively planned in four different centers. Patients with HBsAg positivity for more than six months and HBV-DNA\>2,000 IU/mL, underwent liver biopsy and FibroScan® together within two week. FibroScan® was performed twice, before the antiviral therapy and one year later.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 70 (actual)
- First submitted
- 7 Aug 2024
- Start date
- 2 Jan 2023
- Primary completion date
- 25 Apr 2023
- Lead sponsor
- Yaşar Bayındır, MD
- NCT number
- NCT06573190
What you commit to
- Study type: Observational
- Participants enrolled: 70
- From 2 Jan 2023 to the primary completion date, 25 Apr 2023
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Hepatitis C coinfection
- Hepatitis D and/or HIV coinfections
Other
- Presence of cirrhosis
- Alcohol consumption \>140 g/week in women and 210 g/week in men
Who the study is looking for
- Patients aged 18 years and older with HBsAg positivity for more than six months
- Patients have HBV-DNA level \>2,000 IU/ml for more than six months
Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Güven Hospital Coordinator of this site? Confirm its status | Ankara | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.